Check Your Genetic Health

Mitochondrial Genome Sequencing by NGS

An advanced molecular analysis that examines mitochondrial DNA with high precision to detect genetic mutations causing metabolic disorders, assisting in accurate diagnosis and effective early treatment planning.

Trusted medical contentUpdated: 10-11-2026Views: 0LHL-6437

Frequently Asked Questions

Short answers to the FAQs published with this service.

• What is mitochondrial genome sequencing?

It is an advanced laboratory test that analyzes mitochondrial DNA to detect mutations that may cause genetic diseases related to energy production.

• Does the test require fasting?

No, this analysis does not require fasting, and the blood sample can be collected at any time of the day.

• When will the results be ready?

Due to the complexity of genetic analysis, results typically take between 2 to 4 weeks for the final report to be issued.

• Can the test be done at home?

Yes, home blood collection service for this test is available through our specialized nursing teams.

• Why is NGS technology used?

NGS (Next-Generation Sequencing) allows for the examination of thousands of genetic sequences simultaneously with higher accuracy and speed.

• Who should undergo this test?

It is recommended for individuals with unexplained neurological or muscular symptoms, or when there is a medical suspicion of a mitochondrial disorder.

Medical Laboratories

Check Your Genetic Health

Mitochondrial Genome Sequencing by NGS

Trusted medical contentUpdated: 10-11-2026Views: 0LHL-6437

View service availability

Service typeLaboratory test

Duration15-20 minutes

Fasting / preparationFasting is not required

Home serviceAvailable

Medical notice: this information is for education and service understanding. It is not a diagnosis or a recommendation for an unnecessary procedure.

About this service

A comprehensive genetic test using Next-Generation Sequencing (NGS) to analyze the entire mitochondrial genome, allowing for the precise identification of genetic variants associated with inherited energy and metabolic disorders.

Importance of Testing

Detecting genetic mutations in mitochondrial DNA.
Diagnosing muscle weakness and inherited neurological disorders.
Identifying genetic risks for family members.

Procedure

A simple venous blood sample is collected.
The sample is sent to the lab for DNA extraction.
NGS technology is used to read the full genetic sequence.

Target Groups

Children with unexplained developmental delays.
Patients showing symptoms of metabolic disorders.
Families with a history of mitochondrial diseases.

What is included?

✓Blood sample collection
✓NGS Genetic Analysis
✓Detailed results report

Conditions and notices

Fasting is not required
Providing family medical history
Genetic counseling consultation

Frequently Asked Questions

Short answers to the FAQs published with this service.

• What is mitochondrial genome sequencing?

It is an advanced laboratory test that analyzes mitochondrial DNA to detect mutations that may cause genetic diseases related to energy production.

• Does the test require fasting?

No, this analysis does not require fasting, and the blood sample can be collected at any time of the day.

• When will the results be ready?

Due to the complexity of genetic analysis, results typically take between 2 to 4 weeks for the final report to be issued.

• Can the test be done at home?

Yes, home blood collection service for this test is available through our specialized nursing teams.

• Why is NGS technology used?

NGS (Next-Generation Sequencing) allows for the examination of thousands of genetic sequences simultaneously with higher accuracy and speed.

• Who should undergo this test?

It is recommended for individuals with unexplained neurological or muscular symptoms, or when there is a medical suspicion of a mitochondrial disorder.

Service resources and references

References and additional resources

Reference material and files associated with this service when available.

Scientific references

American College of Medical Genetics
World Health Organization

Service availability

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Content on LahaLak is provided for educational purposes only. It is not a medical diagnosis, prescription, or substitute for consulting a qualified clinician. Medical decisions should not be made from this content alone.

Content reviewed according to the LahaLak Quality Charter.Editorial Policy & Medical Standards

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